All individuals with variants in gene CAPN10

2 entries on 1 page. Showing entries 1 - 2.
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AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

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Age at death     

VIP     

Data_av     

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Disease     

Phenotype details     

Variants     

Panel size     

Owner     
00387869 M9000010 PubMed: Hu 2019 family, 3 affected individuals, first cousin parents - yes - Arab - - - - ID syndromic intellectual disability, microcephaly, epilepsy 1 3 Johan den Dunnen
00387871 M9000033 PubMed: Hu 2019 family, 3 affected individuals, third cousin parents - yes Iran Persia - - - - ID syndromic intellectual disability, microcephaly 1 3 Johan den Dunnen
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